HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172006Generated: October 25, 2026
1,2-Dichloroethane → 3-[(2-Methylprop-2-en-1-yl)oxy]azetidine hydrochloride
https://huagongshe.com/reaction/2172006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-(Diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidine | HCID 67154554 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[(2-Methylprop-2-en-1-yl)oxy]azetidine hydrochloride | HCID 67154496 | — |
Reaction Steps
A 16 mL flask was charged with 1-(diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidine (276 mg, 0.94 mmol; which may be prepared as described in Step 1) and 1,2-dichloroethane (4.1 mL). 1-Chloroethyl chloroformate (135 μL, 1.24 mmol) was added and the reaction mixture was stirred at 70° C. for 1.5 h. After cooling to room temperature, methanol (4.1 mL) was added and the reaction mixture was stirred at 70° C. for 1.5 h. The reaction mixture was concentrated to dryness and the residue was triturated in pentane to give the final product (192 mg, quantitative) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051321B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d2020aa05be84152b2110c3f1814c6f3 |
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| Source note | uspto-grants-2015_06 |
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